| Literature DB >> 27355443 |
Thierry K Slot1, David Eisenberg2, Dylan van Noordenne1, Peter Jungbacker1, Gadi Rothenberg3.
Abstract
The activation of dioxygen for selective oxidation of organic molecules is a major catalytic challenge. Inspired by the activity of nitrogen-doped carbons in electrocatalytic oxygen reduction, we combined such a carbon with metal-oxide catalysts to yield cooperative catalysts. These simple materials boost the catalytic oxidation of several alcohols, using molecular oxygen at atmospheric pressure and low temperature (80 °C). Cobalt and copper oxide demonstrate the highest activities. The high activity and selectivity of these catalysts arises from the cooperative action of their components, as proven by various control experiments and spectroscopic techniques. We propose that the reaction should not be viewed as occurring at an 'active site', but rather at an 'active doughnut'-the volume surrounding the base of a carbon-supported metal-oxide particle.Entities:
Keywords: active sites; cooperative effects; heterogeneous catalysts; oxygen; supported catalysts
Year: 2016 PMID: 27355443 DOI: 10.1002/chem.201602964
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236